rs61750168
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs61750168(C;T) |
Make rs61750168(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 17 |
Position | 8013918 |
Gene | GUCY2D |
is a | snp |
is | mentioned by |
dbSNP | rs61750168 |
dbSNP (classic) | rs61750168 |
ClinGen | rs61750168 |
ebi | rs61750168 |
HLI | rs61750168 |
Exac | rs61750168 |
Gnomad | rs61750168 |
Varsome | rs61750168 |
LitVar | rs61750168 |
Map | rs61750168 |
PheGenI | rs61750168 |
Biobank | rs61750168 |
1000 genomes | rs61750168 |
hgdp | rs61750168 |
ensembl | rs61750168 |
geneview | rs61750168 |
scholar | rs61750168 |
rs61750168 | |
pharmgkb | rs61750168 |
gwascentral | rs61750168 |
openSNP | rs61750168 |
23andMe | rs61750168 |
SNPshot | rs61750168 |
SNPdbe | rs61750168 |
MSV3d | rs61750168 |
GWAS Ctlg | rs61750168 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61750168(G;G) rs61750168(T;T) |
Alt | rs61750168(G;G) rs61750168(T;T) |
Reference | Rs61750168(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GUCY2D |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.7917236C>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000084856.2, |